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This allowed distinguishing annexin V positive cells in early apoptosis, versus annexin V and PI positives cells in late apoptosis or necrosis.
This allowed distinguishing three categories of markers among the 333 polymorphic markers: 174 SSRs that were polymorphic for the A genome (52.0%), 77 SSRs that were polymorphic for the B genome (23.0%) and 82 SSRs that were polymorphic for the two genomes (24.5%).
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This allows distinguishing among markers and to automatically label them [9].
This allows distinguishing the influence of macro- and micro-deformation components on XDP and thereby to extract them separately.
This allows distinguishing between the impacts of various road constructions, as well as sites with different soil properties.
This allows distinguishing each of the possible channel block effects on the APD and ECG.
This allows distinguishing between exons with variability concentrated on third positions versus exons with a more even distribution over the three codon positions.
This allows distinguishing patients with early, active, and late NVC pattern, where the active pattern is defined by the presence of numerous ectasic and giant capillaries (GC), ramified capillaries, micro-haemorrhages (MHE) and micro-thrombosis (MT), and initial loss of capillaries with avascular areas [ 15].
This comparison allows distinguishing between the direct effects of the CMB heterogeneity and the effects of the core evolution.
This axis allows distinguishing rodents living in open and woody areas.
This procedure allows distinguishing enrichments or depletions of specific GO categories in the sample.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com